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Variant : CV613864 (GRCh37/hg19 11q24.2-24.3(chr11:126809705-130289168)) Homo sapiens

Symbol: CV613864
Name: GRCh37/hg19 11q24.2-24.3(chr11:126809705-130289168)
Condition: not provided [RCV000767568]
Clinical Significance: pathogenic
Last Evaluated: 11/01/2018
Review Status: criteria provided, single submitter
Related Genes: ADAMTS8   AP001993.1   APLP2   ARHGAP32   BARX2   C11orf45   ETS1   FLI1   KCNJ1   KCNJ5   KIRREL3   NFRKB   PRDM10   ST14   TMEM45B   TP53AIP1   ZBTB44  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711126,809,705 - 130,289,168CLINVAR
Cytogenetic Map1111q24.2-24.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14399535
Created: 2019-05-07
Species: Homo sapiens
Last Modified: 2020-07-28
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.